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DK1802625T3 - Disubstituted pyrazolobenzodiazepines useful as inhibitors of CDK2 and angiogenesis and in the treatment of breast, colon, lung and prostate cancer - Google Patents

Disubstituted pyrazolobenzodiazepines useful as inhibitors of CDK2 and angiogenesis and in the treatment of breast, colon, lung and prostate cancer

Info

Publication number
DK1802625T3
DK1802625T3 DK05792946T DK05792946T DK1802625T3 DK 1802625 T3 DK1802625 T3 DK 1802625T3 DK 05792946 T DK05792946 T DK 05792946T DK 05792946 T DK05792946 T DK 05792946T DK 1802625 T3 DK1802625 T3 DK 1802625T3
Authority
DK
Denmark
Prior art keywords
cdk2
angiogenesis
colon
breast
lung
Prior art date
Application number
DK05792946T
Other languages
Danish (da)
Inventor
Giacomo Pizzolato
Yi Ren
Kshitij Chhabilbhai Thakkar
Peter Michael Wovkulich
Zhuming Zhang
Jin-Jun Liu
Kin-Chun Luk
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35311946&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DK1802625(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Application granted granted Critical
Publication of DK1802625T3 publication Critical patent/DK1802625T3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/55171,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
DK05792946T 2004-10-13 2005-10-04 Disubstituted pyrazolobenzodiazepines useful as inhibitors of CDK2 and angiogenesis and in the treatment of breast, colon, lung and prostate cancer DK1802625T3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US61817404P 2004-10-13 2004-10-13
PCT/EP2005/010653 WO2006040036A1 (en) 2004-10-13 2005-10-04 Disubstituted pyrazolobenzodiazepines useful as inhibitors for cdk2 and angiogesis, and for the treatment of breast, colon, lung and prostate cancer

Publications (1)

Publication Number Publication Date
DK1802625T3 true DK1802625T3 (en) 2008-09-01

Family

ID=35311946

Family Applications (1)

Application Number Title Priority Date Filing Date
DK05792946T DK1802625T3 (en) 2004-10-13 2005-10-04 Disubstituted pyrazolobenzodiazepines useful as inhibitors of CDK2 and angiogenesis and in the treatment of breast, colon, lung and prostate cancer

Country Status (26)

Country Link
US (1) US7524840B2 (en)
EP (1) EP1802625B1 (en)
JP (1) JP2008515939A (en)
KR (1) KR100858262B1 (en)
CN (2) CN101039946B (en)
AR (1) AR051326A1 (en)
AT (1) ATE398619T1 (en)
AU (1) AU2005293818A1 (en)
BR (1) BRPI0518152A (en)
CA (1) CA2582985A1 (en)
DE (1) DE602005007623D1 (en)
DK (1) DK1802625T3 (en)
ES (1) ES2308551T3 (en)
HK (1) HK1108284A1 (en)
HR (1) HRP20080429T3 (en)
IL (1) IL182423A0 (en)
MX (1) MX2007004464A (en)
NO (1) NO20071794L (en)
NZ (1) NZ554353A (en)
PL (1) PL1802625T3 (en)
PT (1) PT1802625E (en)
RU (1) RU2394826C2 (en)
SI (1) SI1802625T1 (en)
TW (1) TWI309652B (en)
WO (1) WO2006040036A1 (en)
ZA (1) ZA200702973B (en)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2270014A1 (en) 2005-09-22 2011-01-05 Incyte Corporation Azepine inhibitors of janus kinases
BRPI0617252A2 (en) * 2005-10-14 2011-07-19 Hoffmann La Roche administration regimen for benzodiazepine 5-2-chlorophenyl) -1,2-dihydro-7-fluoro-8-methoxy-3-methylpyrazolo [3,4-b] [1,4]
LT2474545T (en) 2005-12-13 2017-02-27 Incyte Holdings Corporation Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as Janus kinase inhibitors
EP3070090B1 (en) 2007-06-13 2018-12-12 Incyte Holdings Corporation Use of salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h- pyrazol-1-yl)-3- cyclopentylpropanenitrile
CL2009001884A1 (en) * 2008-10-02 2010-05-14 Incyte Holdings Corp Use of 3-cyclopentyl-3- [4- (7h-pyrrolo [2,3-d] pyrimidin-4-yl) -1h-pyrazol-1-yl) propanonitrile, janus kinase inhibitor, and use of a composition that understands it for the treatment of dry eye.
KR20100073454A (en) * 2008-12-23 2010-07-01 국립암센터 Novel pyrazolodiazepine compound as an transglutaminase inhibitor, the preparation method thereof and a composition containing the same
UA106078C2 (en) 2009-05-22 2014-07-25 Інсайт Корпорейшн 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- or heptanenitrile as jak inhibitors
NZ596479A (en) 2009-05-22 2014-01-31 Incyte Corp N-(hetero)aryl-pyrrolidine derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines and pyrrol-3-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors
AR078012A1 (en) * 2009-09-01 2011-10-05 Incyte Corp HETEROCICLIC DERIVATIVES OF PIRAZOL-4-IL-PIRROLO (2,3-D) PYRIMIDINS AS INHIBITORS OF THE QUANASA JANUS
EA030376B1 (en) * 2010-03-10 2018-07-31 Инсайт Холдингс Корпорейшн Piperidin-4-yl azetidine derivatives as jak1 inhibitors
JP2011201794A (en) * 2010-03-24 2011-10-13 Fujifilm Corp Process for producing 5-aminopyrazole derivative and salt thereof
KR101921466B1 (en) 2010-05-21 2018-11-26 인사이트 홀딩스 코포레이션 Topical formulation for a jak inhibitor
WO2012068440A1 (en) 2010-11-19 2012-05-24 Incyte Corporation Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors
KR20140019300A (en) 2010-11-19 2014-02-14 인사이트 코포레이션 Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors
EA201490042A1 (en) 2011-06-20 2014-10-30 Инсайт Корпорейшн AZETIDINYL-PHENYL-, PYRIDYL- OR PYRAZYNYLKARBOXAMID DERIVATIVES AS INHIBITORS
TW201313721A (en) 2011-08-18 2013-04-01 Incyte Corp Cyclohexyl azetidine derivatives as JAK inhibitors
UA111854C2 (en) 2011-09-07 2016-06-24 Інсайт Холдінгс Корпорейшн METHODS AND INTERMEDIATE COMPOUNDS FOR JAK INHIBITORS
CN102603743B (en) * 2012-02-24 2014-05-28 南京天易生物科技有限公司 Anti-tumor benzazepine[f]azulene derivative, preparation method thereof, and purpose thereof
TW201406761A (en) 2012-05-18 2014-02-16 Incyte Corp Piperidinylcyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as JAK inhibitors
CN103626761B (en) * 2012-08-24 2015-07-29 上海医药工业研究院 Benazepine compound and the application as antitumor drug thereof
SG10202111768XA (en) 2012-11-15 2021-11-29 Incyte Holdings Corp Sustained-release dosage forms of ruxolitinib
TR201820520T4 (en) 2013-03-06 2019-01-21 Incyte Holdings Corp Processes and intermediates for making a jack inhibitor.
HUE049345T2 (en) 2013-08-07 2020-09-28 Incyte Corp Sustained release dosage forms for a jak1 inhibitor
WO2015184305A1 (en) 2014-05-30 2015-12-03 Incyte Corporation TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1
DK3353177T3 (en) * 2015-09-23 2020-08-24 Janssen Pharmaceutica Nv TRICYCLIC HETEROCYCLES FOR CANCER TREATMENT
HUE057090T2 (en) 2015-09-23 2022-04-28 Janssen Pharmaceutica Nv Bi-heteroaryl substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer
CN106928040A (en) * 2015-12-31 2017-07-07 上海医药工业研究院 The preparation method of SGLT2 inhibitor intermediate
CA3046809A1 (en) * 2016-12-12 2018-06-21 The University Of Sydney Non-peptide oxytocin receptor agonists
RU2723985C9 (en) * 2016-12-13 2020-09-21 Нанкин Транстера Биосайенсиз Ко. Лтд. Multikinase inhibitor compound and its crystalline form and use
CN109020980B (en) * 2017-06-09 2020-11-20 华东师范大学 Pyrazolopyrimidine dinitrogen derivative with anti-tumor effect
US10596161B2 (en) 2017-12-08 2020-03-24 Incyte Corporation Low dose combination therapy for treatment of myeloproliferative neoplasms
RS63312B1 (en) 2018-01-30 2022-07-29 Incyte Corp Processes for preparing (1-(3-fluoro-2-(trifluoromethyl)isonicotinyl)piperidine-4-one)
BR112020019814A2 (en) 2018-03-30 2021-01-05 Incyte Corporation TREATMENT OF SUPURATIVE HYDRADENITIS USING JAK INHIBITORS
US11833155B2 (en) 2020-06-03 2023-12-05 Incyte Corporation Combination therapy for treatment of myeloproliferative neoplasms
AR124154A1 (en) 2020-11-27 2023-02-22 Rhizen Pharmaceuticals Ag CDK INHIBITORS
WO2022149057A1 (en) 2021-01-05 2022-07-14 Rhizen Pharmaceuticals Ag Cdk inhibitors
WO2022236058A1 (en) 2021-05-07 2022-11-10 Kymera Therapeutics, Inc. Cdk2 degraders and uses thereof
KR20240025485A (en) 2022-08-17 2024-02-27 한국화학연구원 Compounds for inhibiting or degrading CDK2 and/or CDK9 and medical uses thereof

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3681341A (en) 1970-12-23 1972-08-01 Hoffmann La Roche Process for preparing 1-lower alkyl-1,4-benzodiazepin-2-ones
US5625031A (en) 1994-02-08 1997-04-29 Bristol-Myers Squibb Company Peptide inhibitors of the p33cdk2 and p34cdc2 cell cycle regulatory kinases and human papillomavirus E7 oncoprotein
US5631156A (en) 1994-06-21 1997-05-20 The University Of Michigan DNA encoding and 18 KD CDK6 inhibiting protein
US5733920A (en) 1995-10-31 1998-03-31 Mitotix, Inc. Inhibitors of cyclin dependent kinases
FR2741881B1 (en) 1995-12-01 1999-07-30 Centre Nat Rech Scient NOVEL PURINE DERIVATIVES HAVING IN PARTICULAR ANTI-PROLIFERATIVE PRORIETES AND THEIR BIOLOGICAL APPLICATIONS
US5866702A (en) 1996-08-02 1999-02-02 Cv Therapeutics, Incorporation Purine inhibitors of cyclin dependent kinase 2
US6440959B1 (en) * 1999-04-21 2002-08-27 Hoffman-La Roche Inc. Pyrazolobenzodiazepines

Also Published As

Publication number Publication date
TW200628469A (en) 2006-08-16
CA2582985A1 (en) 2006-04-20
AR051326A1 (en) 2007-01-03
ATE398619T1 (en) 2008-07-15
NZ554353A (en) 2010-01-29
NO20071794L (en) 2007-07-10
DE602005007623D1 (en) 2008-07-31
ZA200702973B (en) 2009-09-30
AU2005293818A1 (en) 2006-04-20
EP1802625A1 (en) 2007-07-04
PT1802625E (en) 2008-08-06
CN101039946B (en) 2010-12-08
CN101899049A (en) 2010-12-01
RU2007117770A (en) 2008-11-20
KR100858262B1 (en) 2008-09-11
JP2008515939A (en) 2008-05-15
HRP20080429T3 (en) 2008-09-30
MX2007004464A (en) 2007-05-07
CN101039946A (en) 2007-09-19
TWI309652B (en) 2009-05-11
BRPI0518152A (en) 2008-11-04
EP1802625B1 (en) 2008-06-18
IL182423A0 (en) 2007-07-24
PL1802625T3 (en) 2008-12-31
RU2394826C2 (en) 2010-07-20
US7524840B2 (en) 2009-04-28
KR20070054243A (en) 2007-05-28
US20060079511A1 (en) 2006-04-13
ES2308551T3 (en) 2008-12-01
HK1108284A1 (en) 2008-05-02
SI1802625T1 (en) 2008-10-31
WO2006040036A1 (en) 2006-04-20

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